US6191155B1 - Isothiazolcarboxylic acid derivatives - Google Patents

Isothiazolcarboxylic acid derivatives Download PDF

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US6191155B1
US6191155B1 US09/554,170 US55417000A US6191155B1 US 6191155 B1 US6191155 B1 US 6191155B1 US 55417000 A US55417000 A US 55417000A US 6191155 B1 US6191155 B1 US 6191155B1
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carbon atoms
atoms
moiety
halogen
alkyl
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Lutz Assmann
Dietmar Kuhnt
Hans-Ludwig Elbe
Christoph Erdelen
Stefan Dutzmann
Gerd Hänssler
Klaus Stenzel
Astrid Mauler-Machnik
Haruko Sawada
Haruhiko Sakuma
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Bayer AG
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Bayer AG
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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D275/00—Heterocyclic compounds containing 1,2-thiazole or hydrogenated 1,2-thiazole rings
    • C07D275/02—Heterocyclic compounds containing 1,2-thiazole or hydrogenated 1,2-thiazole rings not condensed with other rings
    • C07D275/03—Heterocyclic compounds containing 1,2-thiazole or hydrogenated 1,2-thiazole rings not condensed with other rings with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
    • A01N43/80—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,2
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
    • C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links

Definitions

  • the present invention relates to novel isothiazolecarboxylic acid derivatives, to a process for their preparation and to their use for protecting plants against attack by undesirable microorganisms and animal pests.
  • R represents the groups —OR 1 or —SR 2 in which
  • R 1 represents alkyl having 1 to 12 carbon atoms, where each of these radicals is mono- to trisubstituted by identical or different substituents selected from the group consisting of halogen, cyano, nitro, hydroxyl, carboxyl, alkoxy having 1 to 6 carbon atoms, halogenoalkoxy having 1 to 6 carbon atoms and 1 to 5 halogen atoms, alkylthio having 1 to 6 carbonatoms, halogenoalkylthio having 1 to 6 carbon atoms and 1 to 5 halogen atoms, alkylamino having 1 to 6 carbon atoms, dialkylamino having 1 to 6 carbon atoms in each alkyl moiety, phenylalkoxy having 1 to 4 carbon atoms in the alkoxy moiety and heterocyclylalkoxy having 1 to 3 hetero atoms, such as nitrogen, oxygen and/or sulphur, in the heterocyclyl moiety and 1 to 4 carbon atoms in the alkoxy moiety,
  • R 1 represents aryl having 6 to 10 carbon atoms which may be mono- to trisubstituted by identical or different substituents selected from the group consisting of halogen, cyano, nitro, carboxyl, alkyl having 1 to 6 carbon atoms, halogenoalkyl having 1 to 6 carbon atoms and 1 to 5 halogen atoms, alkoxycarbonyl having 1 to 6 carbon atoms in the alkoxy moiety, alkoxy having 1 to 6 carbon atoms, halogenoalkoxy having 1 to 6 carbon atoms and 1 to 5 halogen atoms, alkylthio having 1 to 6 carbon atoms, halogenoalkylthio having 1 to 6 carbon atoms and 1 to 5 halogen atoms, alkylamino having 1 to 6 carbon atoms, dialkylamino having 1 to 6 carbon atoms in each alkyl moiety, phenyl and phenoxy, or
  • R 1 represents aralkyl having 6 to 10 carbon atoms in the aryl moiety and 1 to 6 carbon atoms in the alkyl moiety, where the aryl moiety may be mono- to trisubstituted by identical or different substituents selected from the group consisting of halogen, cyano, nitro, carboxyl, alkyl having 1 to 6 carbon atoms, halogenoalkyl having 1 to 6 carbon atoms and 1 to 5 halogen atoms, alkoxycarbonyl having 1 to 6 carbon atoms in the alkoxy moiety, alkoxy having 1 to 6 carbon atoms, halogenoalkoxy having 1 to 6 carbon atoms and 1 to 5 halogen atoms, alkylthio having 1 to 6 carbon atoms, halogenoalkylthio having 1 to 6 carbon atoms and 1 to 5 halogen atoms, alkylamino having 1 to 6 carbon atoms, dialkylamino having 1 to 6 carbon atoms in
  • R 1 represents aroxyalkyl having 6 to 10 carbon atoms in the aryl moiety and 1 to 6 carbon atoms in the oxyalkyl moiety, where the aryl moiety may be mono- to trisubstituted by identical or different substituents selected from the group consisting of halogen, cyano, nitro, carboxyl, alkyl having 1 to 6 carbon atoms, halogenoalkyl having 1 to 6 carbon atoms and 1 to 5 halogen atoms, alkoxycarbonyl having 1 to 6 carbon atoms in the alkoxy moiety, alkoxy having 1 to 6 carbon atoms, halogenoalkoxy having 1 to 6 carbon atoms and 1 to 5 halogen atoms, alkylthio having 1 to 6 carbon atoms, halogenoalkylthio having 1 to 6 carbon atoms and 1 to 5 halogen atoms, alkylamino having 1 to 6 carbon atoms, dialkylamino having 1 to 6 carbon atom
  • R 1 represents optionally benzo-fused heterocyclylalkyl having 1 to 3 hetero atoms, such as nitrogen, oxygen and/or sulphur, in the heterocyclyl moiety and 1 to 6 carbon atoms in the alkyl moiety, where the heterocyclyl moiety may be mono- to trisubstituted by identical or different substituents selected from the group consisting of halogen, cyano, nitro, carboxyl, alkyl having 1 to 6 carbon atoms, halogenoalkyl having 1 to 6 carbon atoms and 1 to 5 halogen atoms, alkoxycarbonyl having 1 to 6 carbon atoms in the alkoxy moiety, alkoxy having 1 to 6 carbon atoms, halogenoalkoxy having 1 to 6 carbon atoms and 1 to 5 halogen atoms, alkylthio having 1 to 6 carbon atoms, halogenoalkylthio having 1 to 6 carbon atoms and 1 to 5 halogen atoms, alkyla
  • R 1 represents a radical of the formula
  • n and n independently of one another each represent integers from 1 to 3,
  • R 3 represents alkyl having 1 to 4 carbon atoms or phenyl
  • R 4 represents hydrogen or alkyl having 1 to 4 carbon atoms
  • R 2 represents alkyl having 1 to 12 carbon atoms, where each of these radicals may be mono- to trisubstituted by identical or different substituents selected from the group consisting of halogen, cyano, nitro, carboxyl, alkoxy having 1 to 6 carbon atoms, halogenoalkoxy having 1 to 6 carbon atoms and 1 to 5 halogen atoms, alkylthio having 1 to 6 carbon atoms, halogenoalkylthio having 1 to 6 carbon atoms and 1 to 5 halogen atoms, alkylamino having 1 to 6 carbon atoms, dialkylamino having 1 to 6 carbon atoms in each alkyl moiety, phenylalkoxy having 1 to 4 carbon atoms in the alkoxy moiety and heterocyclylalkoxy having 1 to 3 hetero atoms, such as nitrogen, oxygen and/or sulphur, in the heterocyclyl moiety and 1 to 4 carbon atoms in the alkoxy moiety, or
  • R 2 represents aryl having 6 to 10 carbon atoms which may be mono- to trisubstituted by identical or different substituents selected from the group consisting of halogen, cyano, nitro, carboxyl, alkyl having 1 to 6 carbon atoms, halogenoalkyl having 1 to 6 carbon atoms and 1 to 5 halogen atoms, alkoxycarbonyl having 1 to 6 carbon atoms in the alkoxy moiety, alkoxy having 1 to 6 carbon atoms, halogenoalkoxy having 1 to 6 carbon atoms and 1 to 5 halogen atoms, alkylthio having 1 to 6 carbon atoms, halogenoalkylthio having 1 to 6 carbon atoms, alkylamino having 1 to 6 carbon atoms, dialkylamino having 1 to 6 carbon atoms in each alkyl moiety, phenyl and phenoxy, or
  • R 2 represents aralkyl having 6 to 10 carbon atoms in the aryl moiety and 1 to 6 carbon atoms in the alkyl moiety, where the aryl moiety may be mono- to trisubstituted by identical or different substituents selected from the group consisting of halogen, cyano, nitro, carboxyl, alkyl having 1 to 6 carbon atoms, halogenoalkyl having 1 to 6 carbon atoms and 1 to 5 halogen atoms, alkoxycarbonyl having 1 to 6 carbon atoms in the alkoxy moiety, alkoxy having 1 to 6 carbon atoms, halogenoalkoxy having 1 to 6 carbon atoms and 1 to 5 halogen atoms, alkylthio having 1 to 6 carbon atoms, halogenoalkylthio having 1 to 6 carbon atoms and 1 to 5 halogen atoms, alkylamino having 1 to 6 carbon atoms, dialkylamino having 1 to 6 carbon atoms in
  • R 2 represents aroxyalkyl having 6 to 10 carbon atoms in the aryl moiety and 1 to 6 carbon atoms in the oxyalkyl moiety, where the aryl moiety may be mono- to trisubstituted by identical or different substituents selected from the group consisting of halogen, cyano, nitro, carboxyl, alkyl having 1 to 6 carbon atoms, halogenoalkyl having 1 to 6 carbon atoms and 1 to 5 halogen atoms, alkoxycarbonyl having 1 to 6 carbon atoms in the alkoxy moiety, alkoxy having 1 to 6 carbon atoms, halogenoalkoxy having 1 to 6 carbon atoms and 1 to 5 halogen atoms, alkylthio having 1 to 6 carbon atoms, halogenoalkylthio having 1 to 6 carbon atoms and 1 to 5 halogen atoms, alkylamino having 1 to 6 carbon atoms, dialkylamino having 1 to 6 carbon atom
  • R 2 represents optionally benzo-fused heterocyclylalkyl having 1 to 3 hetero atoms, such as nitrogen, oxygen and/or sulphur, in the heterocyclyl moiety and 1 to 6 carbon atoms in the alkyl moiety, where the heterocyclyl moiety may be mono- to trisubstituted by identical or different substituents selected from the group consisting of halogen, cyano, nitro, carboxyl, alkyl having 1 to 6 carbon atoms, halogenoalkyl having 1 to 6 carbon atoms and 1 to 5 halogen atoms, alkoxycarbonyl having 1 to 6 carbon atoms in the alkoxy moiety, alkoxy having 1 to 6 carbon atoms, halogenoalkoxy having 1 to 6 carbon atoms and 1 to 5 halogen atoms, alkylthio having 1 to 6 carbon atoms, halogenoalkylthio having 1 to 6 carbon atoms and 1 to 5 halogen atoms, alkyla
  • R 2 represents a radical of the formula
  • R 5 represents alkyl having 1 to 4 carbon atoms or phenyl
  • R 6 represents hydrogen or alkyl having 1 to 4 carbon atoms.
  • isothiazolecarboxylic acid derivatives of the formula (I) can be prepared by reacting 3,4-dichloro-isothiazole-5-carbonyl chloride of the formula
  • R is as defined above
  • the isothiazolecarboxylic acid derivatives of the formula (I) are highly suitable for protecting plants against attack by undesirable microorganisms.
  • the compounds according to the invention are suitable both for mobilizing the defences of the plant against attack by undesirable microorganisms and as microbicides for the direct control of microorganisms.
  • the compounds according to the invention are also active against animals which damage plants.
  • the compounds according to the invention have better microbicidal activity than isopropyl 3,4-dichloro-isothiazole-5-carboxylate, which is a constitutionally similar prior-art compound having the same direction of action.
  • the formula (I) provides a general definition of the isothiazolecarboxylic acid derivatives according to the invention. Preference is given to compounds of the formula (I) in which
  • R represents the groups —OR 1 or —SR 2 in which
  • R 1 represents alkyl having 1 to 8 carbon atoms which is mono- to trisubstituted by identical or different substituents selected from the group consisting of fluorine, chlorine, bromine, cyano, nitro, hydroxyl, carboxyl, alkoxy having 1 to 4 carbon atoms, halogenoalkoxy having 1 to 4 carbon atoms and 1 to 3 fluorine, chlorine and/or bromine atoms, alkylthio having 1 to 4 carbon atoms, halogenoalkylthio having 1 to 4 carbon atoms and 1 to 3 fluorine, chlorine and/or bromine atoms, alkylamino having 1 to 4 carbon atoms, dialkylamino having 1 to 4 carbon atoms in each alkyl moiety, phenylalkoxy having 1 or 2 carbon atoms in the alkoxy moiety and five- or six-membered heterocyclylalkoxy having 1 to 3 hetero atoms, such as nitrogen, oxygen and/or sulphur, in the
  • R 1 represents phenyl which may be mono- to trisubstituted by identical or different substituents selected from the group consisting of fluorine, chlorine, bromine, cyano, nitro, carboxyl, alkyl having 1 to 4 carbon atoms, halogenoalkyl having 1 to 4 carbon atoms and 1 to 3 fluorine, chlorine and/or bromine atoms, alkoxycarbonyl having 1 to 4 carbon atoms in the alkoxy moiety, alkoxy having 1 to 4 carbon atoms, halogenoalkoxy having 1 to 4 carbon atoms and 1 to 3 fluorine, chlorine and/or bromine atoms, alkylthio having 1 to 4 carbon atoms, halogenoalkylthio having 1 to 4 carbon atoms and 1 to 3 fluorine, chlorine and/or bromine atoms, alkylamino having 1 to 4 carbon atoms, dialkylamino having 1 to 4 carbon atoms in each alkyl moiety, phenyl and
  • R 1 represents phenylalkyl having 1 to 4 carbon atoms in the alkyl moiety, where the phenyl moiety may be mono- to trisubstituted by identical or different substituents selected from the group consisting of fluorine, chlorine, bromine, cyano, nitro, carboxyl, alkyl having 1 to 4 carbon atoms, halogenoalkyl having 1 to 4 carbon atoms and 1 to 3 fluorine, chlorine and/or bromine atoms, alkoxycarbonyl having 1 to 4 carbon atoms in the alkoxy moiety, alkoxy having 1 to 4 carbon atoms, halogenoalkoxy having 1 to 4 carbon atoms and 1 to 3 fluorine, chlorine and/or bromine atoms, alkylthio having 1 to 4 carbon atoms, halogenoalkylthio having 1 to 4 carbon atoms and 1 to 3 fluorine, chlorine and/or bromine atoms, alkylamino having 1 to 4 carbon atoms,
  • R 1 represents phenoxyalkyl having 1 to 4 carbon atoms in the oxyalkyl moiety, where the phenyl moiety may be mono- to trisubstituted by identical or different substituents selected from the group consisting of fluorine, chlorine, bromine, cyano, nitro, carboxyl, alkyl having 1 to 4 carbon atoms, halogenoalkyl having 1 to 4 carbon atoms and 1 to 3 fluorine, chlorine and/or bromine atoms, alkoxycarbonyl having 1 to 4 carbon atoms in the alkoxy moiety, alkoxy having 1 to 4 carbon atoms, halogenoalkoxy having 1 to 4 carbon atoms and 1 to 3 fluorine, chlorine and/or bromine atoms, alkylthio having 1 to 4 carbon atoms, halogenoalkylthio having 1 to 4 carbon atoms and 1 to 3 fluorine, chlorine and/or bromine atoms, alkylamino having 1 to 4 carbon atoms
  • R 1 represents optionally benzo-fused five- or six-membered heterocyclylalkyl having 1 to 3 hetero atoms, such as nitrogen, oxygen and/or sulphur, in the heterocyclyl moiety and 1 to 4 carbon atoms in the alkyl moiety, where the heterocyclyl moiety may be mono- to trisubstituted by identical or different substituents selected from the group consisting of fluorine, chlorine, bromine, cyano, nitro, carboxyl, alkyl having 1 to 4 carbon atoms, halogenoalkyl having 1 to 4 carbon atoms and 1 to 3 fluorine, chlorine and/or bromine atoms, alkoxycarbonyl having 1 to 4 carbon atoms in the alkoxy moiety, alkoxy having 1 to 4 carbon atoms, halogenoalkoxy having 1 to 4 carbon atoms and 1 to 3 fluorine, chlorine and/or bromine atoms, alkylthio having 1 to 4 carbon atoms, halogeno
  • R 1 represents a radical of the formula
  • n and n independently of one another each represent 1 or 2
  • R 3 represents alkyl having 1 to 3 carbon atoms or phenyl
  • R 4 represents hydrogen or alkyl having 1 to 3 carbon atoms
  • R 2 represents alkyl having 1 to 8 carbon atoms which may be mono- to trisubstituted by identical or different substituents selected from the group consisting of fluorine, chlorine, bromine, cyano, nitro, carboxyl, alkoxy having 1 to 4 carbon atoms, halogenoalkoxy having 1 to 4 carbon atoms and 1 to 3 fluorine, chlorine and/or bromine atoms, alkylthio having 1 to 4 carbon atoms, halogenoalkylthio having 1 to 4 carbon atoms and 1 to 3 fluorine, chlorine and/or bromine atoms, alkylamino having 1 to 4 carbon atoms, dialkylamino having 1 to 4 carbon atoms in each alkyl moiety, phenylalkoxy having 1 or 2 carbon atoms in the alkoxy moiety and five- or six-membered heterocyclylalkoxy having 1 to 3 hetero atoms, such as nitrogen, oxygen and/or sulphur, in the heterocycly
  • R 2 represents phenyl which may be mono- to trisubstituted by identical or different substituents selected from the group consisting of fluorine, chlorine, bromine, cyano, nitro, carboxyl, alkyl having 1 to 4 carbon atoms, halogenoalkyl having 1 to 4 carbon atoms and 1 to 3 fluorine, chlorine and/or bromine atoms, alkoxycarbonyl having 1 to 4 carbon atoms in the alkoxy moiety, alkoxy having 1 to 4 carbon atoms, halogenoalkoxy having 1 to 4 carbon atoms and 1 to 3 fluorine, chlorine and/or bromine atoms, alkylthio having 1 to 4 carbon atoms, halogenoalkylthio having 1 to 4 carbon atoms and 1 to 3 fluorine, chlorine and/or bromine atoms, alkylamino having 1 to 4 carbon atoms, dialkylamino having 1 to 4 carbon atoms in each alkyl moiety, phenyl and
  • R 2 represents phenylalkyl having 1 to 4 carbon atoms in the alkyl moiety, where the phenyl moiety may be mono- to trisubstituted by identical or different substituents selected from the group consisting of fluorine, chlorine, bromine, cyano, nitro, carboxyl, alkyl having 1 to 4 carbon atoms, halogenoalkyl having 1 to 4 carbon atoms and 1 to 3 fluorine, chlorine and/or bromine atoms, alkoxycarbonyl having 1 to 4 carbon atoms in the alkoxy moiety, alkoxy having 1 to 4 carbon atoms, halogenoalkoxy having 1 to 4 carbon atoms and 1 to 3 fluorine, chlorine and/or bromine atoms, alkylthio having 1 to 4 carbon atoms, halogenoalkylthio having 1 to 4 carbon atoms and 1 to 3 fluorine, chlorine and/or bromine atoms, alkylamino having 1 to 4 carbon atoms,
  • R 2 represents phenoxyalkyl having 1 to 4 carbon atoms in the oxyalkyl moiety, where the phenyl moiety may be mono- to trisubstituted by identical or different substituents selected from the group consisting of fluorine, chlorine, bromine, cyano, nitro, carboxyl, alkyl having 1 to 4 carbon atoms, halogenoalkyl having 1 to 4 carbon atoms and 1 to 3 fluorine, chlorine and/or bromine atoms, alkoxycarbonyl having 1 to 4 carbon atoms in the alkoxy moiety, alkoxy having 1 to 4 carbon atoms, halogenoalkoxy having 1 to 4 carbon atoms and 1 to 3 fluorine, chlorine and/or bromine atoms, alkylthio having 1 to 4 carbon atoms, halogenoalkylthio having 1 to 4 carbon atoms and 1 to 3 fluorine, chlorine and/or bromine atoms, alkylamino having 1 to 4 carbon atoms
  • R 2 represents optionally benzo-fused five- or six-membered heterocyclalkyl having 1 to 3 hetero atoms, such as nitrogen, oxygen and/or sulphur, in the heterocyclyl moiety and 1 to 4 carbon atoms in the alkyl moiety, where the heterocyclyl moiety may be mono- to trisubstituted by identical or different substituents selected from the group consisting of fluorine, chlorine, bromine, cyano, nitro, carboxyl, alkyl having 1 to 4 carbon atoms, halogenoalkyl having 1 to 4 carbon atoms and 1 to 3 fluorine, chlorine and/or bromine atoms, alkoxycarbonyl having 1 to 4 carbon atoms in the alkoxy moiety, alkoxy having 1 to 4 carbon atoms, halogenoalkoxy having 1 to 4 carbon atoms and 1 to 3 fluorine, chlorine and/or bromine atoms, alkylthio having 1 to 4 carbon atoms, halogenoalky
  • R 2 represents a radical of the formula
  • R 5 represents alkyl having 1 to 3 carbon atoms or phenyl
  • R 6 represents hydrogen or alkyl having 1 to 3 carbon atoms.
  • R represents the groups —OR 1 or —SR 2 in which
  • R 1 represents alkyl having 1 to 6 carbon atoms which is mono- to trisubstituted by identical or different substituents selected from the group consisting of fluorine, chlorine, bromine, cyano, nitro, hydroxyl, carboxyl, methoxy, ethoxy, isopropoxy, tert-butoxy, halogenoalkoxy having 1 to 3 carbon atoms and 1 to 3 fluorine, chlorine and/or bromine atoms, methylthio, ethylthio, halogenoalkylthio having 1 to 3 carbon atoms and 1 to 3 fluorine, chlorine and/or bromine atoms, methylamino, ethylamino, dimethylamino, diethylamino, benzyloxy or a radical of the formula
  • r 1 or 2
  • R 7 represents pyrrolidinyl, piperidinyl or morpholinyl, or
  • R 1 represents phenyl which may be mono- to trisubstituted by identical or different substituents selected from the group consisting of fluorine, chlorine, bromine, cyano, nitro, carboxyl, methyl, ethyl, propyl, isopropyl, n-butyl, sec-butyl, iso-butyl, tert-butyl, halogenoalkyl having 1 or 2 carbon atoms and 1 to 3 fluorine, chlorine and/or bromine atoms, methoxycarbonyl, ethoxycarbonyl, methoxy, ethoxy, propoxy, isopropoxy, tert-butoxy, halogenoalkoxy having 1 or 2 carbon atoms and 1 to 3 fluorine, chlorine and/or bromine atoms, methylthio, ethylthio, halogenoalkylthio having 1 or 2 carbon atoms and 1 to 3 fluorine, chlorine and/or bromine atoms,
  • R 1 represents phenylalkyl having 1 or 2 carbon atoms in the alkyl moiety, where the phenyl moiety may be mono- to trisubstituted by identical or different substituents selected from the group consisting of fluorine, chlorine, bromine, cyano, nitro, carboxyl, methyl, ethyl, propyl, isopropyl, n-butyl, sec-butyl, iso-butyl, tert-butyl, halogenoalkyl having 1 or 2 carbon atoms and 1 to 3 fluorine, chlorine and/or bromine atoms, methoxycarbonyl, ethoxycarbonyl, methoxy, ethoxy, propoxy, isopropoxy, tert-butoxy, halogenoalkoxy having 1 or 2 carbon atoms and 1 to 3 fluorine, chlorine and/or bromine atoms, methylthio, ethylthio, halogenoalkylthio having
  • R 1 represents phenoxyalkyl having 1 or 2 carbon atoms in the oxyalkyl moiety, where the phenyl moiety may be mono- to trisubstituted by identical or different substituents selected from the group consisting of fluorine, chlorine, bromine, cyano, nitro, carboxyl, methyl, ethyl, propyl, isopropyl, n-butyl, sec-butyl, iso-butyl, tert-butyl, halogenoalkyl having 1 or 2 carbon atoms and 1 to 3 fluorine, chlorine and/or bromine atoms, methoxycarbonyl, ethoxycarbonyl, methoxy, ethoxy, propoxy, isopropoxy, tert-butoxy, halogenoalkoxy having 1 or 2 carbon atoms and 1 to 3 fluorine, chlorine and/or bromine atoms, methylthio, ethylthio, halogenoalkylthio
  • R 1 represents a radical of the formula
  • A represents —CH 2 —, —CH 2 —CH 2 — or
  • R 8 represents pyrazolyl, imidazolyl, 1,2,4-triazolyl, pyrrolyl, furanyl, thienyl, thiazolyl, oxazolyl, pyridinyl, pyrimidinyl, triazinyl, 1,2,3-triazolyl, benzotriazolyl, quinolinyl, isoquinolinyl, quinazolinyl, indolyl, benzothienyl, benzofuranyl, benzothiazolyl or benzimidazolyl, where these radicals may be mono- or disubstituted by identical or different substituents selected from the group consisting of fluorine, chlorine, bromine, cyano, nitro, carboxyl, methyl, ethyl, propyl, isopropyl, n-butyl, sec-butyl, iso-butyl, tert-butyl, halogenoalkyl having 1 or 2 carbon
  • R 1 represents a radical of the formula
  • n and n independently of one another each represent 1 or 2
  • R 3 represents methyl, ethyl or phenyl
  • R 4 represents hydrogen, methyl or ethyl
  • R 2 represents alkyl having 1 to 6 carbon atoms which may be mono- to trisubstituted by identical or different substituents selected from the group consisting of fluorine, chlorine, bromine, cyano, nitro, carboxyl, methoxy, ethoxy, isopropoxy, tert-butoxy, halogenoalkoxy having 1 to 3 carbon atoms and 1 to 3 fluorine, chlorine and/or bromine atoms, methylthio, ethylthio, halogenoalkylthio having 1 to 3 carbon atoms and 1 to 3 fluorine, chlorine and/or bromine atoms, methylamino, ethylamino, dimethylamino, diethylamino, benzyloxy and a radical of the formula
  • s 1 or 2
  • R 9 represents pyrrolidinyl, piperidinyl or morpholinyl, or
  • R 2 represents phenyl which may be mono- to trisubstituted by identical or different substituents selected from the group consisting of fluorine, chlorine, bromine, cyano, nitro, carboxyl, methyl, ethyl, propyl, isopropyl, n-butyl, sec-butyl, isobutyl, tert-butyl, halogenoalkyl having 1 or 2 carbon atoms and 1 to 3 fluorine, chlorine and/or bromine atoms, methoxycarbonyl, ethoxycarbonyl, methoxy, ethoxy, propoxy, isopropoxy, tert-butoxy, halogenoalkoxy having 1 or 2 carbon atoms and 1 to 3 fluorine, chlorine and/or bromine atoms, methylthio, ethylthio, halogenoalkylthio having 1 or 2 carbon atoms and 1 to 3 fluorine, chlorine and/or bromine atoms, methyl
  • R 2 represents phenylalkyl having 1 or 2 carbon atoms in the alkyl moiety, where the phenyl moiety may be mono- to trisubstituted by identical or different substituents selected from the group consisting of fluorine, chlorine, bromine, cyano, nitro, carboxyl, methyl, ethyl, propyl, isopropyl, n-butyl, sec-butyl, iso-butyl, tert-butyl, halogenoalkyl having 1 or 2 carbon atoms and 1 to 3 fluorine, chlorine and/or bromine atoms, methoxycarbonyl, ethoxycarbonyl, methoxy, ethoxy, propoxy, isopropoxy, tert-butoxy, halogenoalkoxy having 1 or 2 carbon atoms and 1 to 3 fluorine, chlorine and/or bromine atoms, methylthio, ethylthio, halogenoalkylthio having
  • R 2 represents phenoxyalkyl having or 2 carbon atoms in the oxyalkyl moiety, where the phenyl moiety may be mono- to trisubstituted by identical or different substituents selected from the group consisting of fluorine, chlorine, bromine, cyano, nitro, carboxyl, methyl, ethyl, propyl, isopropyl, n-butyl, sec-butyl, iso-butyl, tert-butyl, halogenoalkyl having 1 or 2 carbon atoms and 1 to 3 fluorine, chlorine and/or bromine atoms, methoxycarbonyl, ethoxycarbonyl, methoxy, ethoxy, propoxy, isopropoxy, tert-butoxy, halogenoalkoxy having 1 or 2 carbon atoms and 1 to 3 fluorine, chlorine and/or bromine atoms, methylthio, ethylthio, halogenoalkylthio having
  • R 2 represents a radical of the formula
  • a 1 represents —CH 2 —, —CH 2 —CH 2 — or
  • R 10 represents pyrazolyl, imidazolyl, 1,2,4-triazolyl, pyrrolyl, furanyl, thienyl, thiazolyl, oxazolyl, pyridinyl, pyrimidinyl, triazinyl, 1,2,3-triazolyl, benzotriazolyl, quinolinyl, iso-quinolinyl, quinazolinyl, indolyl, benzothienyl, benzofuranyl, benzothiazolyl or benzimidazolyl, where these radicals may be mono- or disubstituted by identical or different substituents selected from the group consisting of fluorine, chlorine, bromine, cyano, nitro, carboxyl, methyl, ethyl, propyl, isopropyl, n-butyl, sec-butyl, iso-butyl, tert-butyl, halogenoalkyl having 1 or 2 carbon
  • R 2 represents a radical of the formula
  • R 5 represents methyl, ethyl or phenyl
  • R 6 represents hydrogen, methyl or ethyl.
  • the formula (III) provides a general definition of the alcohols and thioalcohols furthermore required as reaction components for carrying out the process according to the invention.
  • R preferably and in particular has those meanings which have already been mentioned in connection with the description of the substances of the formula (D according to the invention as being preferred and as being particularly preferred, respectively, for this radical.
  • Suitable acid binders for carrying out the process according to the invention are all customary inorganic or organic bases.
  • Suitable diluents for carrying out the process according to the invention are all inert organic solvents. Preference is given to using aliphatic, alicyclic or aromatic hydrocarbons, such as petroleum ether, hexane, heptane, cyclohexane, methyl cyclohexane, benzene, toluene, xylene or decalin; halogenated hydrocarbons, such as chlorobenzene, dichlorobenzene, dichloromethane, chloroform, carbon tetrachloride, dichloroethane or trichloroethane; ethers, such as diethyl ether, diisopropyl ether, methyl t-butyl ether, methyl t-amyl ether, dioxane, tetrahydrofuran, 1,2-dimethoxyethane, 1,2-diethoxyethane or anisole; nitriles, such as aceton
  • reaction temperatures can be varied within a relatively wide range.
  • the reaction is carried out at temperatures between ⁇ 10° C. and +150° C., preferably between 0° C. and 100° C.
  • the process according to the invention is generally carried out under atmospheric pressure. However, it is also possible to carry out the process under elevated or, if no volatile components participate in the reaction, under reduced pressure.
  • the active compounds according to the invention have a potent plant-strengthening action. They are therefore suitable for mobilizing the defences of the plant against attack by undesirable microorganisms.
  • plant-strengthening compounds are those substances which are capable of stimulating the defensive system of plants in such a way that the treated plants, when subsequently inoculated with undesirable microorganisms, develop substantial resistance against these microorganisms.
  • undesirable microorganisms are phytopathogenic fungi, bacteria and viruses.
  • the compounds according to the invention can also be used to protect plants within a certain period of time after the treatment against attack by the abovementioned harmful organisms.
  • the period of time for which protection is effected generally extends for from 1 to 10 days, preferably for 1 to 7 days, after the treatment of the plants with the active compounds.
  • the active compounds according to the invention also have potent microbicidal action and are additionally used in practice for directly controlling undesirable microorganisms.
  • the active compounds are suitable for use as crop protection agents, in particular as fungicides.
  • the undesirable microorganisms include fungi from the classes of the Plasmodiophoromycetes, Oomycetes, Chytridiomycetes, Zygomycetes, Ascomycetes, Basidiomycetes, Deuteromycetes.
  • Pythium species such as, for example, Pythium ultimum
  • Phytophthora species such as, for example, Phytophthora infestans
  • Pseudoperonospora species such as, for example, Pseudoperonospora humuli or Pseudoperonospora cubensis;
  • Plasmopara species such as, for example, Plasmopara viticola
  • Peronospora species such as, for example, Peronospora pisi or Peronospora brassicae;
  • Erysiphe species such as, for example, Erysiphe graminis
  • Sphaerotheca species such as, for example, Sphaerotheca fuliginea
  • Podosphaera species such as, for example, Podosphaera leucotricha
  • Venturia species such as, for example, Venturia inaequalis
  • Pyrenophora species such as, for example, Pyrenophora teres or Pyrenophora graminea (Conidia form: Drechslera, syn: Helminthosporium);
  • Cochliobolus species such as, for example, Cochliobolus sativus (Conidia form: Drechslera, syn: Helminthosporium);
  • Uromyces species such as, for example, Uromyces appendiculatus
  • Puccinia species such as, for example, Puccinia recondita
  • Tilletia species such as, for example, Tilletia caries
  • Ustilago species such as, for example, Ustilago nuda or Ustilago avenae;
  • Pellicularia species such as, for example, Pellicularia sasakii;
  • Pyricularia species such as, for example, Pyricularia oryzae
  • Fusarium species such as, for example, Fusarium culmorum
  • Botrytis species such as, for example, Botrytis cinerea
  • Septoria species such as, for example, Septoria nodorum
  • Leptosphaeria species such as, for example, Leptosphaeria nodorum;
  • Cercospora species such as, for example, Cercospora canescens
  • Altemaria species such as, for example, Alternaria brassicae;
  • Pseudocercosporella species such as, for example, Pseudocercosporella herpotrichoides.
  • the good crop safety of the active compounds at the concentrations required for controlling plant diseases permits a treatment of above-ground parts of plants, and also a treatment of propagation stock and seed and of the soil.
  • the active compounds according to the invention can be used here particularly successfully for controlling cereal diseases, such as, for example, against Erysiphe species, or of diseases in viticulture, fruit and vegetable growing, such as, for example, against Plasmopara or Venturia species, or of rice diseases, such as, for example, against Pyricularia species.
  • the active compounds according to the invention also permit successful control of other plant diseases, such as, for example, Septoria, Cochliobolus, Pyrenophora and Pseudocercosporella species, and specific mention may be made of Drechslera teres.
  • the active compounds according to the invention are also suitable for increasing the harvest yield. Additionally, they have reduced toxicity and good crop safety.
  • the active compounds according to the invention are also suitable for controlling animal pests, in particular insects, arachnids and nematodes, which are encountered in agriculture, in forests, in horticulture, in the protection of stored products and of materials, and also in the hygiene field and in veterinary medicine, and have good crop safety and favourable toxicity to warm-blooded animals.
  • the compounds are active against normally sensitive and resistant species and against pests in all or some stages of development.
  • the abovementioned pests include:
  • Chilopoda for example, Geophilus carpophagus and Scutigera spec.
  • Symphyla for example, Scutigerella immaculata.
  • Thysanura for example, Lepisma saccharina.
  • Orthoptera for example, Blatta orientalis, Periplaneta americana, Leucophaea maderae, Blattella germanica, Acheta domesticus, Gryllotalpa spp., Locusta migratoria migratorioides, Melanoplus differentialis and Schistocerca gregaria.
  • Thysanoptera From the order of the Thysanoptera, for example, Hercinothrips femoralis and Thrips tabaci.
  • From the order of the Homoptera for example, Aleurodes brassicae, Bemisia tabaci, Trialeurodes vaporariorum, Aphis gossypii, Brevicoryne brassicae, Cryptomyzus ribis, Aphis fabae, Aphis pomi, Eriosoma lanigerum, Hyalopterus arundinis, Phylloxera vastatrix, Pemphigus spp., Macrosiphum avenae, Myzus spp., Phorodon humuli, Rhopalosiphum padi, Empoasca spp., Euscelis bilobatus, Nephotettix cincticeps, Lecanium corni, Saissetia oleae, Laodelphax striatellus, Nilaparvata lugens, Aonidiella aurantii, Aspidiotus hederae, Pseu
  • Hymenoptera From the order of the Hymenoptera, for example, Diprion spp., Hoplocampa spp., Lasius spp., Monomorium pharaonis and Vespa spp.
  • Acarina for example, Acarus siro, Argas spp., Ornithodoros spp., Dermanyssus gallinae, Eriophyes ribis, Phyllocoptruta oleivora, Boophilus spp., Rhipicephalus spp., Amblyomma spp., Hyalonmma spp., Ixodes spp., Psoroptes spp., Chorioptes spp., Sarcoptes spp., Tarsonemus spp., Bryobia praetiosa, Panonychus spp. and Tetranychus spp.
  • the phytoparasitic nematodes include, for example, Pratylenchus spp., Radopholus similis, Ditylenchus dipsaci, Tylenchulus serrmipenetrans, Heterodera spp., Globodera spp., Meloidogyne spp., Aphelenchoides spp., Longidorus spp., Xiphinema spp. and Trichodorus spp.
  • the compounds according to the invention can be employed particularly successfully for controlling plant-damaging mites, such as against the greenhouse red spider mite ( Tetranychus urticae ), or for controlling plant-damraging insects, such as against the caterpillars of the diamond-back moth ( Plutella maculipennis ), the larvae of the mustard beetle ( Phaedon cochleariae ), and the green rice leafhopper ( Nephotettix cincticeps ).
  • plant-damaging mites such as against the greenhouse red spider mite ( Tetranychus urticae )
  • plant-damraging insects such as against the caterpillars of the diamond-back moth ( Plutella maculipennis ), the larvae of the mustard beetle ( Phaedon cochleariae ), and the green rice leafhopper ( Nephotettix cincticeps ).
  • the compounds according to the invention also have herbicidal activity.
  • the active compounds can be converted to the customary formulations, such as solutions, emulsions, suspensions, powders, foams, pastes, granules, aerosols, very fine capsules in polymeric substances and in coating compositions for seed, and also ULV cold- and warm-fogging formulations.
  • customary formulations such as solutions, emulsions, suspensions, powders, foams, pastes, granules, aerosols, very fine capsules in polymeric substances and in coating compositions for seed, and also ULV cold- and warm-fogging formulations.
  • formulations are produced in a known manner, for example by mixing the active compounds with extenders, that is, liquid solvents, liquefied pressurized gases and/or solid carriers, optionally with the use of surface-active agents, that is emulsifying agents and/or dispersing agents, and/or foam-forming agents. If the extender used is water, it is also possible to employ for example organic solvents as auxiliary solvents.
  • extenders that is, liquid solvents, liquefied pressurized gases and/or solid carriers
  • surface-active agents that is emulsifying agents and/or dispersing agents, and/or foam-forming agents.
  • the extender used is water, it is also possible to employ for example organic solvents as auxiliary solvents.
  • Suitable liquid solvents are essentially: aromatics, such as xylene, toluene or alkylnaphthalenes, chlorinated aromatics or chlorinated aliphatic hydrocarbons, such as chlorobenzenes, chloroethylenes or methylene chloride, aliphatic hydrocarbons, such as cyclohexane or paraffins, for example mineral oil fractions, alcohols, such as butanol or glycol as well as their ethers and esters, ketones, such as acetone, methyl ethyl ketone, methyl isobutyl ketone or cyclohexanone, strongly polar solvents, such as dimethylformamide and dimethyl sulphoxide, and also water.
  • aromatics such as xylene, toluene or alkylnaphthalenes
  • chlorinated aromatics or chlorinated aliphatic hydrocarbons such as chlorobenzenes, chloroethylenes or methylene chloride
  • Liquefied gaseous extenders or carriers are those liquids which are gaseous at ambient temperature and at atmospheric pressure, for example aerosol propellants such as halogenated hydrocarbons and also butane, propane, nitrogen and carbon dioxide.
  • aerosol propellants such as halogenated hydrocarbons and also butane, propane, nitrogen and carbon dioxide.
  • solid carriers there are suitable: for example ground natural minerals, such as kaolins, clays, talc, chalk, quartz, attapulgite, montmorillonite or diatomaceous earth, and ground synthetic minerals, such as finely divided silica, alumina and silicates.
  • solid carriers for granules there are suitable: for example crushed and fractionated natural rocks such as calcite, marble, pumice, sepiolite and dolomite, and also synthetic granules of inorganic and organic meals, and granules of organic material such as sawdust, coconut shells, maize cobs and tobacco stalks.
  • emulsifying and/or foam-forming agents there are suitable: for example non-ionic and anionic emulsifiers, such as polyoxyethylene fatty acid esters, polyoxyethylene fatty alcohol ethers, for example alkylaryl polyglycol ethers, alkylsulphonates, alkyl sulphates, arylsulphonates and also protein hydrolysates.
  • dispersing agents there are suitable: for example lignin-sulphite waste liquors and methylcellulose.
  • Tackifiers such as carboxymethylcellulose and natural and synthetic polymers in the form of powders, granules or latices, such as gum arabic, polyvinyl alcohol and polyvinyl acetate, as well as natural phospholipids, such as cephalins and lecithins, and synthetic phospholipids, can be used in the formulations.
  • Other possible additives are mineral and vegetable oils.
  • colorants such as inorganic pigments, for example iron oxide, titanium oxide and Prussian Blue, and organic dyestuffs, such as alizarin dyestuffs, azo dyestuffs and metal phthalocyanine dyestuffs, and trace nutrients such as salts of iron, manganese, boron, copper, cobalt, molybdenum and zinc.
  • organic dyestuffs such as alizarin dyestuffs, azo dyestuffs and metal phthalocyanine dyestuffs
  • trace nutrients such as salts of iron, manganese, boron, copper, cobalt, molybdenum and zinc.
  • the formulations in general contain between 0.1 and 95% by weight of active compound, preferably between 0.5 and 90%.
  • the active compounds according to the invention can be used as such or in their formulations, also as a mixture with known fungicides, bactericides, acaricides, nematicides, or insecticides, for example, to improve the activity spectrum or prevent the development of resistance. In many instances, synergistic effects are obtained, i.e. the activity of the mixture exceeds the activity of the individual components.
  • aldimorph ampropylfos, ampropylfos potassium, andoprim, anilazine, azaconazole, azoxystrobin,
  • debacarb debacarb, dichlorophen, diclobutrazole, diclofluanid, diclomezine, dicloran, diethofencarb, difenoconazole, dimethirimol, dimethomorph, diniconazole, diniconazole-M, dinocap, diphenylamine, dipyrithione, ditalimfos, dithianon, dodemorph, dodine, drazoxolon,
  • kasugamycin kasugamycin, kresoxim-methyl
  • copper preparations such as: copper hydroxide, copper naphthenate, copper oxychloride, copper sulphate, copper oxide, oxine-copper and Bordeaux mixture,
  • paclobutrazole pefurazoate, penconazole, pencycuron, phosdiphen, pimaricin, piperalin, polyoxin, polyoxorim, probenazole, prochloraz, procyrridone, propamocarb, propanosine-sodium, propiconazole, propineb, pyrazophos, pyrifenox, pyrimethanil, pyroquilon, pyroxyfur,
  • tebuconazole tecloftalam, tecnazene, tetcyclasis, tetraconazole, thiabendazole, thicyofen, thifluzamide, thiophanate-methyl, thiram, tioxymid, tolclofos-methyl, tolylfluanid, triadimefon, triadimenol, triazbutil, triazoxide, trichlamide, tricyclazole, tridemorph, triflumizole, triforine, triticonazole,
  • Bacillus thuringiensis 4-bromo-2-(4-chlorophenyl)-1-(ethoxymethyl)-5-(trifluoromethyl)-1H-pyrrole-3-carbonitrile, bendiocarb, benfuracarb, bensultap, betacyfluthrin, bifenthrin, BPMC, brofenprox, bromophos A, bufencarb, buprofezin, butocarboxim, butylpyridaben,
  • edifenphos emamectin, esfenvalerat, ethiofencarb, ethion, ethofenprox, ethoprophos, etrimphos,
  • fenamiphos fenazaquin, fenbutatin oxide, fenitrothion, fenobucarb, fenothiocarb, fenoxycarb, fenpropathrin, fenpyrad, fenpyroximat, fenthion, fenvalerate, fipronil, fluazinam, fluazuron, flucycloxuron, flucythrinate, flufenoxuron, flufenprox, fluvalinate, fonophos, formothion, fosthiazate, fubfenprox, furathiocarb,
  • parathion A parathion M, permethrin, phenthoate, phorate, phosalone, phosmet, phosphamidon, phoxim, pirimicarb, pirimiphos M, pirimiphos A, profenofos, promecarb, propaphos, propoxur, prothiofos, prothoat, pymetrozin, pyrachlophos, pyridaphenthion, pyresmethrin, pyrethrum, pyridaben, pyrimidifen, pyriproxifen,
  • vamidothion XMC, xylylcarb, zetamethrin.
  • the active compounds can be used as such, in the form of their formulations or the use forms prepared therefrom, such as ready-to-use solutions, suspensions, wettable powders, pastes, soluble powders, dusts and granules.
  • Application is carried out in a customary manner, for example by watering, spraying, atomizing, scattering, dusting, foaming, spreading, etc.
  • the application rates can be varied within a relatively wide range, depending on the kind of application.
  • the active compound application rates are generally between 0.1 and 10,000 g/ha, preferably between 10 and 1000 g/ha.
  • the active compound application rates are generally between 0.001 and 50 g per kilogram of seed, preferably between 0.01 and 10 g per kilogram of seed.
  • the active compound application rates are generally between 0.1 and 10,000 g/ha, preferably between 1 and 5000 g/ha.
  • the compounds according to the invention when used against animal pests, can be present in commercially available formulations and also in the use forms prepared from these formulations as a mixture with synergists.
  • Synergists are compounds which increase the activity of the active compounds, without it being necessary for the added synergist itself to be active.
  • the active compound content of the use forms prepared from the commercial formulations can vary within wide ranges.
  • the active compound concentration of the use forms may be from 0.0000001 to 95% by weight of active compound, preferably between 0.0001 and 1% by weight.
  • the application is carried out in a manner which is adapted to the use forms.
  • the phases are separated and the aqueous phase is extracted once more with 300 ml of ethyl acetate.
  • the combined organic phases are initially washed with 450 ml of aqueous sodium bicarbonate solution and then with 300 ml of aqueous sodium chloride solution and then concentrated under reduced pressure.
  • the product that remains is admixed with ethyl acetate.
  • the resulting precipitate is filtered off with suction and dried. This gives 1.17 g of a crystalline product of melting point 127 to 129° C.
  • Emulsifier 0.06 parts by weight of alkylaryl polyglycol ether
  • active compound 1 part by weight of active compound is mixed with the stated amount of solvent, and the concentrate is diluted with water and the stated amount of emulsifier to the desired concentration.
  • Evaluation is carried out 4 days after the inoculation. 0% means an efficacy which corresponds to that of the control, while an efficacy of 100% means that no infection is observed.
  • Emulsifier 1 part by weight of alkylaryl polyglycol ether
  • active compound 1 part by weight of active compound is mixed with the stated amounts of solvent and emulsifier, and the concentrate is diluted with water to the desired concentration.
  • Cabbage leaves Brassica oleracea
  • Cabbage leaves Brassica oleracea
  • Emulsifier 0.6 parts by weight of alkylaryl polyglycol ether
  • active compound 1 part by weight of active compound is mixed with the stated amounts of solvent and emulsifier, and the concentrate is diluted with water to the desired concentration.
  • the plants are placed in a greenhouse at a temperature of approximately 20° C. and a relative atmospheric humidity of approximately 80% to promote the development of mildew pustules.
  • Evaluation is carried out 7 days after the inoculation. 0% means an efficacy which corresponds to that of the control, while an efficacy of 100% means that no infection is observed.
  • Emulsifier 0.6 parts by weight of alkylaryl polyglycol ether
  • active compound 1 part by weight of active compound is mixed with the stated amounts of solvent and emulsifier, and the concentrate is diluted with water to the desired concentration.
  • the plants are placed in a greenhouse at a temperature or approximately 15° C. and a relative atmospheric humidity of 80%.
  • Evaluation is carried out 10 days after the inoculation. 0% means an efficacy which corresponds to that of the control, while an efficacy of 100% means that no infection is observed.

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DE19750011A DE19750011A1 (de) 1997-11-12 1997-11-12 Isothiazolcarbonsäure-Derivate
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US20100227900A1 (en) * 2009-02-03 2010-09-09 Bayer Cropscience Ag Use of Sulphur-Containing Heteroaromatic Acid Analogues as Bactericides
US20100311580A1 (en) * 2007-12-11 2010-12-09 Bayer Cropscience Ag Active Compound Combinations
US20150011394A1 (en) * 2012-01-21 2015-01-08 Bayer Intellectual Property Gmbh Use of host defense inducers for controlling bacterial harmful organisms in useful plants
US8951934B2 (en) 2008-12-19 2015-02-10 Bayer Cropscience Ag Active compound combinations
US20150291540A1 (en) * 2012-10-05 2015-10-15 Ihara Chemical Industry Co., Ltd. Method for manufacturing isothiazole compound

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JP2001122864A (ja) * 1999-10-20 2001-05-08 Nippon Bayer Agrochem Co Ltd イソチアゾールカルボン酸誘導体
JP2001213869A (ja) * 2000-01-28 2001-08-07 Nippon Bayer Agrochem Co Ltd イソチアゾールカルボン酸誘導体および病害防除剤
JP2001294581A (ja) * 2000-04-12 2001-10-23 Nippon Bayer Agrochem Co Ltd イソチアゾール誘導体
JP2003113167A (ja) * 2001-10-05 2003-04-18 Bayer Ag イソチアゾール類および病害防除剤
JP2003146975A (ja) * 2001-11-15 2003-05-21 Bayer Ag イソチアゾール類および病害防除剤
EP2070413A1 (en) 2007-12-11 2009-06-17 Bayer CropScience AG Active compound combinations
EP2070415A1 (en) 2007-12-11 2009-06-17 Bayer CropScience AG Active compound combinations
EP2070411A1 (en) 2007-12-11 2009-06-17 Bayer CropScience AG Active compound combinations
JP6027442B2 (ja) 2009-10-15 2016-11-16 バイエル・クロップサイエンス・アクチェンゲゼルシャフト 活性化合物の組み合わせ
CN102942565B (zh) * 2012-11-06 2016-01-27 江西天人生态股份有限公司 一类3,4-二氯异噻唑衍生物及其制备方法和用途
AR093996A1 (es) 2012-12-18 2015-07-01 Bayer Cropscience Ag Combinaciones bactericidas y fungicidas binarias
WO2017178407A1 (en) 2016-04-13 2017-10-19 Bayer Cropscience Aktiengesellschaft Fungicidal combinations
CN108031305A (zh) * 2017-12-23 2018-05-15 刘顶康 一种延长聚烯烃微滤膜抗菌持久性的方法

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US5240951A (en) * 1990-09-20 1993-08-31 Mitsui Toatsu Chemicals, Incorporated Isothiazolecarboxylic acid derivatives, rice blast control agents containing the same as active ingredients, and rice blast control method applying the control agents
JPH069313A (ja) 1992-06-29 1994-01-18 Mitsui Toatsu Chem Inc イソチアゾールカルボン酸アニリド誘導体を有効成分とするイネいもち病防除剤
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US20100311580A1 (en) * 2007-12-11 2010-12-09 Bayer Cropscience Ag Active Compound Combinations
US8951934B2 (en) 2008-12-19 2015-02-10 Bayer Cropscience Ag Active compound combinations
US20100227900A1 (en) * 2009-02-03 2010-09-09 Bayer Cropscience Ag Use of Sulphur-Containing Heteroaromatic Acid Analogues as Bactericides
KR20110118804A (ko) * 2009-02-03 2011-11-01 바이엘 크롭사이언스 아게 살균제로서의 황-함유 헤테로방향족산 유사체의 용도
US20150011394A1 (en) * 2012-01-21 2015-01-08 Bayer Intellectual Property Gmbh Use of host defense inducers for controlling bacterial harmful organisms in useful plants
US20150291540A1 (en) * 2012-10-05 2015-10-15 Ihara Chemical Industry Co., Ltd. Method for manufacturing isothiazole compound
US9353071B2 (en) * 2012-10-05 2016-05-31 Ihara Chemical Industry Co., Ltd. Method for manufacturing isothiazole compound

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AR016008A1 (es) 2001-05-30
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WO1999024414A1 (de) 1999-05-20
EP1044195A1 (de) 2000-10-18
CO5040010A1 (es) 2001-05-29
JP4511720B2 (ja) 2010-07-28
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BR9814134A (pt) 2000-10-03
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